84753-03-7 Usage
Uses
Used in Surfactant and Detergent Production:
2-hydroxyhexadecyl dihydrogen phosphate is used as a surfactant and detergent ingredient for its ability to reduce surface tension and enhance solubility, which improves the cleaning and emulsifying properties of these products.
Used in Lubricant Production:
2-hydroxyhexadecyl dihydrogen phosphate is used as a lubricant additive for its ability to reduce friction and wear, improving the performance and longevity of lubricated systems.
Used in Cosmetic and Personal Care Products:
2-hydroxyhexadecyl dihydrogen phosphate is used as an emulsifier in various cosmetic and personal care products, helping to stabilize mixtures of oil and water, and improving the texture and feel of the products.
Used in Pharmaceutical Applications:
2-hydroxyhexadecyl dihydrogen phosphate has been studied for its potential pharmaceutical applications, particularly in the formulation of drug delivery systems and as an adjuvant in vaccine formulations. Its ability to enhance solubility and reduce surface tension may contribute to improved drug delivery and vaccine efficacy.
However, the potential environmental and health effects of 2-hydroxyhexadecyl dihydrogen phosphate are still under investigation, and caution is advised in its handling and use.
Check Digit Verification of cas no
The CAS Registry Mumber 84753-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84753-03:
(7*8)+(6*4)+(5*7)+(4*5)+(3*3)+(2*0)+(1*3)=147
147 % 10 = 7
So 84753-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H35O5P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16(17)15-21-22(18,19)20/h16-17H,2-15H2,1H3,(H2,18,19,20)
84753-03-7Relevant academic research and scientific papers
Osanai, Shuichi,Yamada, Go,Hidano, Ruri,Beppu, Koji,Namiwa, Kimiyoshi
, p. 41 - 49 (2010)
Phosphate surfactants containing ether and hydroxyl groups were prepared by a simple reaction between the corresponding epoxide and the diethyl phosphate. The relationships between the structure and colloidal properties were evaluated in terms of the critical micelle concentration (CMC), γCMC, foaming ability, and water absorbing and holding abilities. Based on these results, it was concluded that the ether and hydroxy groups synergistically worked together to decrease the CMC and increase the foaming ability. The degree of neutralization remarkably affected the colloidal properties. The highly neutralized states showed a more positive effect on water holding power but an opposite effect on the foaming ability. Copyright
